Palladium catalyzed bicyclization of 1,8-diiodonaphthalene and tertiary propargylic alcohols to phenalenones and their applications as fluorescent chemosensor for fluoride ions

Chem Commun (Camb). 2011 Mar 7;47(9):2628-30. doi: 10.1039/c0cc04875e. Epub 2011 Jan 13.

Abstract

Phenalenone derivatives were efficiently constructed from 1,8-diiodonaphthalene and tertiary propynols via a one-pot domino reaction which eventually included Pd-catalyzed Sonogoshira coupling, Pd-catalyzed allylic oxidation and Pd-catalyzed C(sp(2))-H activation. Moreover, the synthesized phenalenone derivative presented a practical application as a fluorescent chemosensor for fluoride anion with high sensitivity and selectivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Catalysis
  • Cyclization
  • Fluorides / analysis*
  • Ions / chemistry
  • Naphthalenes / chemistry*
  • Oxidation-Reduction
  • Palladium / chemistry*
  • Phenalenes / chemistry*
  • Propanols / chemistry*
  • Solvents / chemistry
  • Temperature

Substances

  • Alkynes
  • Ions
  • Naphthalenes
  • Phenalenes
  • Propanols
  • Solvents
  • naphthalene
  • phenalen-1-one
  • Palladium
  • propargyl alcohol
  • Fluorides